MuscleSport Test Revolution™ is the most advanced natural testosterone enhancing product to date. Where other test boosters fall short, Test Revolution™ delivers!
This powerful formula helps support increases in circulating testosterone while also blocking the body’s production of estrogen by using powerful, clinically studied key ingredients such as:
- Fenutest™ Fenugreek - Supports increases in circulating testosterone.
- Testafuranol™ Tribulus - Assists in elevating luteinizing hormone levels.
- Peruvian Maca - Supports increased Libido
Test Revolution™ is clearly the Alpha of all testosterone boosters. When you really want help increasing your body’s natural testosterone levels, you want proven ingredients that boost test safely and effectively.
The comprehensive ingredient profile found in Test Revolution™ will assist in maximizing natural testosterone output and promote a superior muscle building environment.
*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
FREE TESTOSTERONE MATRIX
Tribulus is an herb that is mostly recommended for male health including virility and vitality, and specifically more catered towards cardiovascular and urogenital health.
- It is a common supplement for its libido enhancing properties and testosterone boosting properties.
- The theory behind tribulus is it elevates luteinizing hormone, which in turn sends instructions to the testes causing them to make testosterone.
- Sellandi et al. (2012) found in men supplementing with tribulus for 60 days were able to increase testosterone by 16.3%.
Trigonella foenum-graecum, commonly known as fenugreek, is a popular herb in Arabic regions and India. It has traditionally been used to enhance libido and masculinity.
- A human study done by Wilborn et al. (2010) noted that fenugreek supplementation led to increases in testosterone and bio-available testosterone, while also decreasing body fat.
Fadogia Agrestis Extract
Fadogia Agretis may help increase testosterone levels and lower estrogen levels at the same time.
- A University of Ilorin study on Fadogia Agrestis showed an incredible 200% increase in testosterone over the course of 5 days. Increases in libido and strength were also noted by the researchers..
Maca is a plant in the broccoli family. Maca has traditionally been used as an aphrodisiac.
Magnesium is an essential mineral and electrolyte. It is involved in protein synthesis, ATP formation, metabolism of carbohydrates and fats, and bone strength.
- Magnesium deficiencies are the second most common deficiency in developed countries. A lack of magnesium will raise blood pressure and reduce insulin sensitivity.
- Increases in free and total testosterone have been noted in sedentary and athletic populations when supplementing with magnesium supplementation. It also acts as a muscle relaxer and may improve aerobic performance.
- Brilla et al. (1992) discovered 26 untrained subjects who participated in a 7-week strength training program in conjunction with magnesium supplementation were able to increase testosterone relative to baseline.
Zinc is vital for several important physiological roles in the body and is needed for many enzymatic reactions including those necessary to stimulate muscle protein synthesis.
- Zinc deficiency has been linked to low IGF-1 Levels and Growth Hormone.
- Zinc also supports optimal testosterone levels and may increase testosterone at rest and after exercise.
- A 2006 study by Killic et al. found wrestlers who supplemented with Zinc for 4 weeks were able to preserve circulating testosterone and thyroid hormone concentrations, which declined in placebo due to the exhaustive workload.
B6 is a water soluble vitamin that is important to various metabolic reactions that occur in the body. It is also a coenzyme for protein metabolism and the nervous and immune system function.
- B6 is also involved in the synthesis of hormones and red blood cells.
- Vitamin B6 may have some benefits with regard to increasing the rate of synthesis of testosterone.
- B6 may also be able to increase levels of growth hormone.
ESTRO BLOCK MATRIX
DIM is a molecule that consists of two indole groups attached to a methine group. It is commonly found in broccoli and holds promise as an aromatase inhibitor.
- DIM has potent effects on estrogen metabolism and is able to keep the body relatively balanced by preventing either drastic increases or decreases in estrogen.
Saw Palmetto Berry Extract
Saw Palmetto is a fatty acid mix from Serenoa repens that may increase testosterone and suppress prostate growth.
Q: What is the best way to take Test Revolution?
A: As a dietary supplement, take one serving (3 capsules) of Test Revolution in the morning with 8-10oz of water. For optimal performance take an additional serving in the evening.
Q: Do natural testosterone boosters really work?
A: Yes, depending upon the right ingredients being used. The ingredients in Test Revolution have been confirmed by research to boost natural testosterone levels.
Q: Who do you recommend should take Test Revolution?
A: Test Revolution should be taken by older individuals, individuals with lower than normal testosterone levels, and athletes/younger (18-29 years) individuals who may need a temporary increase in testosterone production to break through training plateaus.
Q: What other MuscleSport products do you recommend stacking with Test Revolution?
1. Brown, G. A., Vukovich, M. D., Sharp, R. L., Reifenrath, T. A., Parsons, K. A., & King, D. S. (1999). Effect of oral DHEA on serum testosterone and adaptations to resistance training in young men. Journal of Applied Physiology, 87(6), 2274-2283.
2. Brown, G. A., Vukovich, M. D., Martini, E. R., Kohut, M. L., Franke, W. D., Jackson, D. A., & King, D. S. (2001). Effects of androstenedione-herbal supplementation on serum sex hormone concentrations in 30-to 59-year-old men. International journal for vitamin and nutrition research, 71(5), 293-301.
3. Brown, G. A., Vukovich, M. D., Martini, E. R., Kohut, M. L., Franke, W. D., Jackson, D. A., & King, D. S. (2001). Endocrine and lipid responses to chronic androstenediol-herbal supplementation in 30 to 58 year old men.Journal of the American College of Nutrition, 20(5), 520-528.
4. Sellandi, T. M., Thakar, A. B., & Baghel, M. S. (2012). Clinical study of Tribulus terrestris Linn. in Oligozoospermia: A double blind study. Ayu, 33(3), 356.
5. Dimitrov, M., Georgiev, P., & Vitanov, S. (1986). [Use of tribestan on rams with sexual disorders]. Veterinarno-meditsinski nauki, 24(5), 102-110.
1. Chevassus, H., Molinier, N., Costa, F., Galtier, F., Renard, E., & Petit, P. (2009). A fenugreek seed extract selectively reduces spontaneous fat consumption in healthy volunteers. European journal of clinical pharmacology, 65(12), 1175-1178.
2. Wilborn, C., Taylor, L., Poole, C., Foster, C., Willoughby, D., & Kreider, R. (2010). Effects of a Purported Aromatase and 5 α-Reductase Inhibitor on Hormone Profiles in College-Age Men. International journal of sport nutrition,20(6), 457.
3. Steels, E., Rao, A., & Vitetta, L. (2011). Physiological Aspects of Male Libido Enhanced by Standardized Trigonella foenum‐graecum Extract and Mineral Formulation. Phytotherapy Research, 25(9), 1294-1300.
4. Kochhar, A., & Nagi, M. (2005). Effect of supplementation of traditional medicinal plants on blood glucose in non-insulin-dependent diabetics: a pilot study. Journal of medicinal food, 8(4), 545-549.
5. Gupta, A., Gupta, R., & Lal, B. (2001). Effect of Trigonella foenum-graecum (fenugreek) seeds on glycaemic control and insulin resistance in type 2 diabetes mellitus: a double blind placebo controlled study. The Journal of the Association of Physicians of India, 49, 1057-1061.
Fadogia Agrestis Extract
1. Yakubu, M. T., Akanji, M. A., & Oladiji, A. T. (2005). Aphrodisiac potentials of the aqueous extract of Fadogia agrestis (Schweinf. Ex Hiern) stem in male albino rats. Asian Journal of Andrology, 7(4), 399-404.
1. Brooks, N. A., Wilcox, G., Walker, K. Z., Ashton, J. F., Cox, M. B., & Stojanovska, L. (2008). Beneficial effects of Lepidium meyenii (Maca) on psychological symptoms and measures of sexual dysfunction in postmenopausal women are not related to estrogen or androgen content.Menopause, 15(6), 1157-1162.
2. Gonzales, G. F., Cordova, A., Vega, K., Chung, A., Villena, A., Góñez, C., & Castillo, S. (2002). Effect of Lepidium meyenii (MACA) on sexual desire and its absent relationship with serum testosterone levels in adult healthy men.andrologia, 34(6), 367-372.
3. Zenico, T., Cicero, A. F. G., Valmorri, L., Mercuriali, M., & Bercovich, E. (2009). Subjective effects of Lepidium meyenii (Maca) extract on well‐being and sexual performances in patients with mild erectile dysfunction: a randomised, double‐blind clinical trial. Andrologia, 41(2), 95-99.
4. Dording, C. M., Fisher, L., Papakostas, G., Farabaugh, A., Sonawalla, S., Fava, M., & Mischoulon, D. (2008). A Double‐Blind, Randomized, Pilot Dose‐Finding Study of Maca Root (L. Meyenii) for the Management of SSRI‐Induced Sexual Dysfunction. CNS Neuroscience & Therapeutics, 14(3), 182-191.
1. Cinar, V., Polat, Y., Baltaci, A. K., & Mogulkoc, R. (2011). Effects of magnesium supplementation on testosterone levels of athletes and sedentary subjects at rest and after exhaustion. Biological trace element research, 140(1), 18-23.
2. van der Plas, A. A., Schilder, J. C., Marinus, J., & van Hilten, J. J. (2013). An explanatory study evaluating the muscle relaxant effects of intramuscular magnesium sulphate for dystonia in complex regional pain syndrome. The Journal of Pain, 14(11), 1341-1348.
3. Hatzistavri, L. S., Sarafidis, P. A., Georgianos, P. I., Tziolas, I. M., Aroditis, C. P., Zebekakis, P. E., ... & Lasaridis, A. N. (2009). Oral magnesium supplementation reduces ambulatory blood pressure in patients with mild hypertension. American journal of hypertension, 22(10), 1070-1075.
4. Golf, S. W., Bender, S., & Grüttner, J. (1998). On the significance of magnesium in extreme physical stress. Cardiovascular Drugs and Therapy,12(2), 197-202.
5. Carpenter, T. O., DeLucia, M. C., Zhang, J. H., Bejnerowicz, G., Tartamella, L., Dziura, J., ... & Cohen, D. (2006). A randomized controlled study of effects of dietary magnesium oxide supplementation on bone mineral content in healthy girls. The Journal of Clinical Endocrinology & Metabolism, 91(12), 4866-4872.
6. Held, K., Antonijevic, I. A., Künzel, H., Uhr, M., Wetter, T. C., Golly, I. C., ... & Murck, H. (2002). Oral Mg (2+) supplementation reverses age-related neuroendocrine and sleep EEG changes in humans. Pharmacopsychiatry,35(4), 135-143.
7. Brilla, L. R., & Haley, T. F. (1992). Effect of magnesium supplementation on strength training in humans. Journal of the American College of Nutrition,11(3), 326-329.
1. Brilla, L. R., & Conte, V. (2000). Effects of a novel zinc-magnesium formulation on hormones and strength. J Exerc Physiol Online, 3(4), 26-36.
2. Kilic, M., Baltaci, A. K., Gunay, M., Gökbel, H., Okudan, N., & Cicioglu, I. (2005). The effect of exhaustion exercise on thyroid hormones and testosterone levels of elite athletes receiving oral zinc. Neuro endocrinology letters, 27(1-2), 247-252.
3. Kilic, M. (2007). Effect of fatiguing bicycle exercise on thyroid hormone and testosterone levels in sedentary males supplemented with oral zinc. Neuro endocrinology letters, 28(5), 681-685.
4. Jalali, G. R., Roozbeh, J., Mohammadzadeh, A., Sharifian, M., Sagheb, M. M., Jahromi, A. H., ... & Afshariani, R. (2010). Impact of oral zinc therapy on the level of sex hormones in male patients on hemodialysis. Renal failure,32(4), 417-419.
5. Netter, A., Nahoul, K., & Hartoma, R. (1981). Effect of zinc administration on plasma testosterone, dihydrotestosterone, and sperm count. Archives of Andrology, 7(1), 69-73.
6. Tupe, R. P., & Chiplonkar, S. A. (2009). Zinc supplementation improved cognitive performance and taste acuity in Indian adolescent girls. Journal of the American College of Nutrition, 28(4), 388-396.
7. Prasad, A. S., Beck, F. W., Bao, B., Fitzgerald, J. T., Snell, D. C., Steinberg, J. D., & Cardozo, L. J. (2007). Zinc supplementation decreases incidence of infections in the elderly: effect of zinc on generation of cytokines and oxidative stress. The American journal of clinical nutrition,85(3), 837-844.
1. Moretti, C., Fabbri, A., Gnessi, L., Bonifacio, V., Fraioli, F., & Isidori, A. (1982). Pyridoxine (B6) suppresses the rise in prolactin and increases the rise in growth hormone induced by exercise. The New England journal of medicine, 307(7), 444.
1. Lo, R., & Matthews, J. (2010). A New Class of Estrogen Receptor Beta–Selective Activators. Molecular interventions, 10(3), 133.
2. Leong, H., Riby, J. E., Firestone, G. L., & Bjeldanes, L. F. (2004). Potent ligand-independent estrogen receptor activation by 3, 3′-diindolylmethane is mediated by cross talk between the protein kinase A and mitogen-activated protein kinase signaling pathways. Molecular Endocrinology, 18(2), 291-302.
3. Leong, H., Firestone, G. L., & Bjeldanes, L. F. (2001). Cytostatic effects of 3, 3′-diindolylmethane in human endometrial cancer cells result from an estrogen receptor-mediated increase in transforming growth factor-α expression. Carcinogenesis, 22(11), 1809-1817.
4. Sanderson, J. T., Slobbe, L., Lansbergen, G. W., Safe, S., & Van den Berg, M. (2001). 2, 3, 7, 8-Tetrachlorodibenzo-p-dioxin and diindolylmethanes differentially induce cytochrome P450 1A1, 1B1, and 19 in H295R human adrenocortical carcinoma cells. Toxicological sciences, 61(1), 40-48.
5. Safe, S., Wang, F., Porter, W., Duan, R., & McDougal, A. (1998). Ah receptor agonists as endocrine disruptors: antiestrogenic activity and mechanisms. Toxicology letters, 102, 343-347.
Pygeum Africanum Extract
1. Wilt, T., Ishani, A., Mac Donald, R., Rutks, I., & Stark, G. (1998). Pygeum africanum for benign prostatic hyperplasia. Cochrane database of systematic reviews,
2. Yablonsky, F., Nicolas, V., Riffaud, J. P., & Bellamy, F. (1997). Antiproliferative effect of Pygeum africanum extract on rat prostatic fibroblasts. The Journal of urology, 157(6), 2381-2387.
3. Bombardelli, E., & Morazzoni, P. (1997). Prunus africana (Hook. f.) Kalkm.Fitoterapia, 68(3), 205-218.
4. Barlet, A., Albrecht, J., Aubert, A., Fischer, M., Grof, F., Grothuesmann, H. G., ... & Reichelt, H. (1990). [Efficacy of Pygeum africanum extract in the medical therapy of urination disorders due to benign prostatic hyperplasia: evaluation of objective and subjective parameters. A placebo-controlled double-blind multicenter study]. Wiener Klinische Wochenschrift, 102(22), 667-673.
5. Menchini-Fabris, G. F., Giorgi, P., Andreini, F., Canale, D., Paoli, R., & Sarteschi, M. L. (1988). [New perspectives on the use of Pygeum Africanum in prostato-bladder pathology]. Archivio italiano di urologia, nefrologia, andrologia: organo ufficiale dell'Associazione per la ricerca in urologia= Urological, nephrological, and andrological sciences, 60(3), 313-322.
Saw Palmetto Berry Extract
1. Bertaccini, A., Giampaoli, M., Cividini, R., Gattoni, G. L., Sanseverino, R., Realfonso, T., ... & Galasso, R. (2012). Observational database serenoa repens (DOSSER): overview, analysis and results. A multicentric SIUrO (Italian Society of Oncological Urology) project. Archivio italiano di urologia, andrologia: organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica/Associazione ricerche in urologia, 84(3), 117-122.
2. Suter, A., Saller, R., Riedi, E., & Heinrich, M. (2013). Improving BPH symptoms and sexual dysfunctions with a saw palmetto preparation? Results from a pilot trial. Phytotherapy Research, 27(2), 218-226.
3. Gerber, G. S., Kuznetsov, D., Johnson, B. C., & Burstein, J. D. (2001). Randomized, double-blind, placebo-controlled trial of saw palmetto in men with lower urinary tract symptoms. Urology, 58(6), 960-963.
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